Echocardiographic findings in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia.
نویسندگان
چکیده
1. Konstam, M. Heart failure training. J Am Coll Cardiol 2004;44: 1361–2. 2. Naccarelli GV. Does it make sense to train plumbers as electricians? J Am Coll Cardiol 2004;44:1358–60. 3. McAlister FA, Steward S, Ferrua S, McMurray JJJ. Multidisciplinary strategies for the management of heart failure patients at high risk for admission. A systematic review of randomized trials. J Am Coll Cardiol 2004;44:810–9.
منابع مشابه
Pathologic evidence of extensive left ventricular involvement in arrhythmogenic right ventricular cardiomyopathy.
Arrhythmogenic right ventricular cardiomyopathy (also known as arrhythmogenic right ventricular dysplasia) is characterized by adipose or fibroadipose tissue replacement of the right ventricular myocardium, whereas the left ventricle is substantively spared. Two cases of the disease with evidence of extensive left ventricular involvement at pathologic examination are described. Hearts from two ...
متن کاملMRI of arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Magnetic Resonance Imaging (MRI) is currently considered as the noninvasive modality of choice for evaluation of patients with suspected Arrhythmogenic Right Ventricular Dysplasia (i.e., right ventricular dysplasia). As arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) it is included in the WHO classification of cardiomyopathies. It has the unique ability to provide tissue char...
متن کاملDilated Cardiomyopathy Hypertrophic Cardiomyopathy Arrhythmogenic right ventricular dysplasia Restrictive Cardiomyopathy Idiopathic Secondary Amyloidosis2 Loeffler's eosinophilic endocardial fibrosis2 Tropical endocardial fibrosis (Davies disease) Unclassified cardiomyopathies Mitochondrial cardiomyopathy Fibroelastosis Noncompacted myocardium Systolic dysfunction with minimal dilatation3
Definition and Classification The cardiomyopathies are a diverse group of myocardial diseases that are characterized by chronic ventricular dysfunction. The clinical classification of cardiomyopathy is based on hemodynamic and echocardiographic abnormalities, and consists of dilated cardiomyopathy, hypertrophic cardiomyopathy, and restrictive cardiomyopathy. Recently, arrhythmogenic right ventr...
متن کاملPredictors of adverse outcome in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy: long term experience of a tertiary care centre.
OBJECTIVE To investigate the predictors for adverse clinical outcome in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) during long term follow up. METHODS 61 patients with ARVD/C were studied to assess the impact of family history, clinical findings, surface ECG parameters, echocardiographic findings, and electrophysiological findings on clinical outcome. The...
متن کاملElectrocardiographic features of disease progression in arrhythmogenic right ventricular cardiomyopathy/dysplasia
BACKGROUND Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is considered a progressive cardiomyopathy. However, data on the clinical features of disease progression are limited. The aim of this study was to assess 12-lead surface electrocardiographic (ECG) changes during long-term follow-up, and to compare these findings with echocardiographic data in our large cohort of pati...
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ورودعنوان ژورنال:
- Journal of the American College of Cardiology
دوره 46 10 شماره
صفحات -
تاریخ انتشار 2005